Article
VPS33B mutation with ichthyosis, cholestasis, and renal dysfunction but without arthrogryposis: incomplete ARC syndrome phenotype.
The Journal of pediatrics - 1 Feb 2006
Bull Laura N, Mahmoodi Venus, Baker Alastair J, Jones Rosamond, Strautnieks Sandra S, Thompson Richard J, Knisely A S
Abstract excerpt
Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome is a rare multisystem disorder first described in 1979 and recently ascribed to mutation in VPS33B, whose product acts in intracellular trafficking. Arthrogryposis, spillage of various substances in the urine, and conjugated hyperbilirubinemia define an ARC core phenotype, in some patients associated with ichthyosis, central nervous system malformation,...
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